LanceSoft
Job Title: Quality Auditor Associate
Location: 575 South Chipeta Way, Salt Lake City, UT 84108
Duration: 4-5 Months
1st shift early (6 a.m. - 2:30 p.m. M-F)
Description: The job requirements include the following essential areas of responsibility:
Perform sampling and delivery of intermediate and finished products. Assist with retain sample management. Conduct monthly GMP and batch-specific room audits. Perform in process record review of commercial manufacturing batch records. Review completed swab data and perform subsequent room/equipment release. Ensures compliance with all Company policies and procedures, including safety rules and regulations. Performs related duties as assigned. Education/Certification/Experience:
Requires a minimum of one year experience in a regulated environment such as pharmaceutical, medical device, nutraceutical, or food processing industries. Requires basic understanding of Good Manufacturing Practice (cGMP) and the application to a production environment. Associate's degree or higher (or equivalent) achieved or in process preferred. Skills/Knowledge/Abilities:
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems. Self-directed with ability to organize and prioritize work Ability to communicate effectively with excellent written and oral communication skills Ability to interact positively and collaborate with co-workers and management
1st shift early (6 a.m. - 2:30 p.m. M-F)
Description: The job requirements include the following essential areas of responsibility:
Perform sampling and delivery of intermediate and finished products. Assist with retain sample management. Conduct monthly GMP and batch-specific room audits. Perform in process record review of commercial manufacturing batch records. Review completed swab data and perform subsequent room/equipment release. Ensures compliance with all Company policies and procedures, including safety rules and regulations. Performs related duties as assigned. Education/Certification/Experience:
Requires a minimum of one year experience in a regulated environment such as pharmaceutical, medical device, nutraceutical, or food processing industries. Requires basic understanding of Good Manufacturing Practice (cGMP) and the application to a production environment. Associate's degree or higher (or equivalent) achieved or in process preferred. Skills/Knowledge/Abilities:
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), EDMS and ERP systems. Self-directed with ability to organize and prioritize work Ability to communicate effectively with excellent written and oral communication skills Ability to interact positively and collaborate with co-workers and management